ENST00000261769.10:c.1734A>G
MANE Select
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ENSP00000261769.4:p.Thr578=
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ENST00000261769.9:c.1734A>G
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ENSP00000261769.4:p.Thr578=
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ENST00000422392.6:c.1551A>G
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ENSP00000414946.2:p.Thr517=
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ENST00000562836.5:n.1805A>G
|
|
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ENST00000566510.5:c.*400A>G
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ENSP00000458139.1:n.*400A>G
|
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ENST00000566612.5:c.1588A>G
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ENSP00000454782.1:p.Arg530Gly
|
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ENST00000611625.4:c.1797A>G
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ENSP00000481063.1:p.Thr599=
|
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ENST00000612417.4:c.1734A>G
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ENSP00000478360.1:p.Thr578=
|
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ENST00000621016.4:c.1734A>G
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ENSP00000480664.1:p.Thr578=
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NM_004360.3:c.1734A>G , LRG_301t1:c.1734A>G
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NP_004351.1:p.Thr578=
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XM_011523488.1:c.999A>G
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XP_011521790.1:p.Thr333=
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XM_011523489.1:c.999A>G
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XP_011521791.1:p.Thr333=
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NM_001317184.1:c.1551A>G
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NP_001304113.1:p.Thr517=
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NM_001317185.1:c.186A>G
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NP_001304114.1:p.Thr62=
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NM_001317186.1:c.-232A>G
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NP_001304115.1:n.-232A>G
|
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NM_004360.4:c.1734A>G
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NP_004351.1:p.Thr578=
|
|
NM_004360.5:c.1734A>G
MANE Select
|
NP_004351.1:p.Thr578=
|
|
NM_001317184.2:c.1551A>G
|
NP_001304113.1:p.Thr517=
|
|
NM_001317185.2:c.186A>G
|
NP_001304114.1:p.Thr62=
|
|
NM_001317186.2:c.-232A>G
|
NP_001304115.1:n.-232A>G
|
|